Host-pathogen interaction of human coronaviruses - interferon induction

Pathway network for the Host-pathogen interaction of human coronaviruses - interferon induction SuperPath

Sources:
  • WikiPathways
  • PharmGKB

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Host-pathogen interaction of human coronaviruses - interferon induction SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Multisystem inflammatory syndrome in childrenEnrichmentIFIH1, IFNAR2, IFNB1, IRF3, TRAF310.53
2Herpes simplex virus encephalitisEnrichmentTBK1, TLR3, TRAF37.21
3Singleton-merten syndromeEnrichmentIFIH1, RIGI6.00
4Immunodeficiency 44EnrichmentIFNAR2, STAT25.53
5Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA5.24
6Hepatitis bEnrichmentIFNAR2, IL10RB4.82
7Immunodeficiency 68EnrichmentMYD883.43
8Macroglobulinemia, waldenstrom 1EnrichmentMYD883.43
9Encephalopathy, acute, infection-induced 7EnrichmentIRF33.43
10Macular degeneration, age-related, 10EnrichmentTLR43.43
11Waldenstram macroglobulinemiaEnrichmentMYD883.43
12Transient predisposition to invasive pyogenic bacterial infectionEnrichmentMYD883.13
13Immunodeficiency 35EnrichmentTYK22.99
14Singleton-merten syndrome 1EnrichmentIFIH12.99
15Encephalopathy, acute, infection-induced 6EnrichmentTICAM12.99
16Pseudo-torch syndrome 3EnrichmentSTAT22.99
17Immunodeficiency 106 viral infectionsEnrichmentIFNAR12.99
18Immunodeficiency 95EnrichmentIFIH12.99
19Immunodeficiency 132aEnrichmentTRAF32.99
20Type 1 diabetes mellitus 19EnrichmentIFIH12.99
21Immunodeficiency 132bEnrichmentTRAF32.99
22Immunodeficiency 31aEnrichmentSTAT12.99
23Immunodeficiency 31bEnrichmentSTAT12.99
24Singleton-merten syndrome 2EnrichmentRIGI2.99
25Immunodeficiency 65 viral infectionsEnrichmentIRF92.99
26Aicardi-goutieres syndrome 7EnrichmentIFIH12.99
27Dermatitis, atopic, 4EnrichmentSOCS32.79
28Immunodeficiency 39 viral infectionsEnrichmentIRF72.79
29Leukoencephalopathy, developmental delay, and episodic neurologic regression syndromeEnrichmentEIF2AK22.79
30Immunodeficiency 39EnrichmentIRF72.79
31Immunodeficiency 100 with pulmonary alveolar proteinosis and hypogammaglobulinemiaEnrichmentOAS12.79
32Dystonia 33EnrichmentEIF2AK22.79
33Pseudo-torch syndrome 2EnrichmentUSP182.79
34Infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemiaEnrichmentOAS12.79
35Adar-related hereditary spastic paraplegiaEnrichmentADAR2.79
36Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK12.79
37Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF62.73
38Leprosy 3EnrichmentTLR22.72
39Immunodeficiency 83 viral infectionsEnrichmentTLR32.72
40Immunodeficiency 74, covid19-related, x-linkedEnrichmentTLR72.72
41X-linked immunodeficiency 74EnrichmentTLR72.72
42Systemic lupus erythematosus 17EnrichmentTLR72.72
43Autoinflammation with arthritis and vasculitisEnrichmentTBK12.72
44Corticobasal syndromeEnrichmentTBK12.72
45Encephalopathy, acute, infection-induced 8EnrichmentTBK12.72
46Immunodeficiency 45EnrichmentIFNAR22.69
47Immunodeficiency 31cEnrichmentSTAT12.69
48Lymphomatoid papulosisEnrichmentTYK22.69
49Basal ganglia diseaseEnrichmentIFIH12.69
50Primary cutaneous anaplastic large cell lymphomaEnrichmentTYK22.69
51Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.61
52Incontinentia pigmentiEnrichmentIKBKG2.61
53Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.61
54Fetal encasement syndromeEnrichmentCHUK2.61
55Frontometaphyseal dysplasia 2EnrichmentMAP3K72.61
56Immunodeficiency 15bEnrichmentIKBKB2.61
57Immunodeficiency 15aEnrichmentIKBKB2.61
58Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.61
59Bartsocas-papas syndrome 2EnrichmentCHUK2.61
60Autoinflammation with episodic fever and lymphadenopathyEnrichmentRIPK12.61
61Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.61
62Dyschromatosis symmetrica hereditariaEnrichmentADAR2.49
63Aicardi-goutieres syndrome 6EnrichmentADAR2.49
64Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK12.49
65Symmetrical dyschromatosis of extremitiesEnrichmentADAR2.49
66Frontotemporal dementia and/or amyotrophic lateral sclerosis 4EnrichmentTBK12.42
67Leprosy 1EnrichmentTLR62.42
68Hepatitis c virusEnrichmentIFNL32.31
69Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK12.31
70Torsion dystonia 1EnrichmentEIF2AK22.31
71Inflammatory bowel disease 25EnrichmentIL10RB2.31
72Immunodeficiency 33EnrichmentIKBKG2.31
73Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.31
74Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.31
75Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.31
76Immunodeficiency 57 with autoinflammationEnrichmentRIPK12.31
77Common variable immunodeficiency 12EnrichmentNFKB12.31
78Spastic diplegiaEnrichmentIFIH12.29
79Chronic mucocutaneous candidiasisEnrichmentSTAT12.21
80Familial infantile bilateral striatal necrosisEnrichmentADAR2.19
81Behcet syndromeEnrichmentTLR42.16
82Diffuse large b-cell lymphomaEnrichmentMYD882.16
83Nasopharyngeal carcinomaEnrichmentNFKBIA2.14
84Frontometaphyseal dysplasiaEnrichmentMAP3K72.14
85Aicardi-goutiares syndromeEnrichmentIFIH12.03
86Inflammatory bowel disease 25, autosomal recessiveEnrichmentIL10RB2.01
87Il10-related early-onset inflammatory bowel diseaseEnrichmentIL10RB2.01
88Congenital generalized lipodystrophyEnrichmentFOS2.01
89Aicardi-goutieres syndromeEnrichmentIFIH11.99
90Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.92
91Histiocytoid hemangiomaEnrichmentFOS1.92
92Motor neuron diseaseEnrichmentTBK11.87
93Common variable immunodeficiencyEnrichmentNFKB11.77
94Progressive non-fluent aphasiaEnrichmentTBK11.77
95Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentTBK11.72
96Coronary heart disease 5EnrichmentIKBKG1.66
97Ciliary dyskinesia, primary, 3EnrichmentNFKB11.62
98Immune deficiency diseaseEnrichmentRIPK11.58
99Human immunodeficiency virus type 1EnrichmentTLR31.47
100GliosarcomaEnrichmentNFKBIA1.42
101Giant cell glioblastomaEnrichmentNFKBIA1.39
102Severe covid-19EnrichmentIL10RB1.34
103NephronophthisisEnrichmentPIAS11.28
104MalariaEnrichmentIKBKG1.26
105Systemic lupus erythematosusEnrichmentTLR71.14
106Severe combined immunodeficiencyEnrichmentIKBKB1.11
107Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentTBK10.98
108Hereditary breast ovarian cancer syndromeEnrichmentRIPK10.90
109Colorectal cancerEnrichmentADAR0.88
110Breast cancerEnrichmentJUN0.78

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